ChemicalBook Product Catalog Chemical Reagents Organic reagents Esters Methyl ester compound Dimethyl 5-hydroxyisophthalate

Dimethyl 5-hydroxyisophthalate

Dimethyl 5-hydroxyisophthalate Basic information
Product Name:Dimethyl 5-hydroxyisophthalate
Synonyms:3-benzenedicarboxylicacid,5-hydroxy-dimethylester;TIMTEC-BB SBB000491;DIMETHYL-5-HYDROXY-BENZENE-1,3-DICARBONATE;DIMETHYL 5-HYDROXYBENZENE-1,3-DICARBOXYLATE;DIMETHYL 5-HYDROXYISOPHTHALATE;5-HYDROXYISOPHTHALIC ACID DIMETHYL ESTER;Dimethyl 5-hydroxybenzene-1,3-dicarboxylate~5-Hydroxyisophthalic acid dimethyl ester;Dimethyl 5-hydroxyisophtalate
CAS:13036-02-7
MF:C10H10O5
MW:210.18
EINECS:235-899-0
Product Categories:Acids & Esters;Phenols;Aromatic Esters
Mol File:13036-02-7.mol
Dimethyl 5-hydroxyisophthalate Structure
Dimethyl 5-hydroxyisophthalate Chemical Properties
Melting point 162-164 °C (lit.)
Boiling point 360.6±22.0 °C(Predicted)
density 1.284±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
solubility DMSO (Slightly), Methanol (Slightly)
form Powder and/or Lumps
pka8.33±0.10(Predicted)
color White to light beige
Water Solubility Soluble in water.
BRN 2650120
InChIKeyDOSDTCPDBPRFHQ-UHFFFAOYSA-N
LogP2.570 (est)
CAS DataBase Reference13036-02-7(CAS DataBase Reference)
EPA Substance Registry SystemDimethyl 5-hydroxyisophthalate (13036-02-7)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-36-37/39
WGK Germany 3
TSCA Yes
HS Code 29182900
MSDS Information
ProviderLanguage
ACROS English
SigmaAldrich English
ALFA English
Dimethyl 5-hydroxyisophthalate Usage And Synthesis
Chemical Propertiesoff-white crystal powder
UsesDimethyl 5-Hydroxyisophthalate is a useful synthetic intermediate in the synthesis of N,N?-Bis(2,3-dihydroxypropyl)-5-[(N-(2-hydroxyethyl)carbamoyl)methoxy]-2,4,6-triiodoisophthalamide (B426310); a compound related to Ioversol( I737000) which is a nonionic, low osmolality, radiographic contrast agent.
General DescriptionDimethyl 5-hydroxyisophthalate undergoes a base-catalyzed nucleophilic oxirane ring-opening addition reaction with allyl glycidyl ether, to afford 5-substituted derivatives of isophthalic acid. Influence of third component, i.e. a series of 1,ω-alkanediols on the copolymerization reaction of dimethyl 5-hydroxyisophthalate with poly(ethylene glycol) has been studied. Lipase-catalyzed condensation polymerization of dimethyl 5-hydroxyisophthalate with polyethylene glycol is reported.
Dimethyl 5-hydroxyisophthalate Preparation Products And Raw materials
Preparation ProductsMETHYL 3-FORMYL-5-METHOXYBENZOATE-->3,5-BIS(TRIFLUOROMETHYL)ANISOLE-->1,3-Benzenedicarboxylic acid, 5-hydroxy-4-(2-propen-1-yl)-, 1,3-dimethyl ester-->5-(naphthalen-1-ylmethoxy)isophthalic acid-->Tert-Butyl7-oxo-3-azabicyclo[3.3.1]nonane-3-carboxylate-->METHYL 4-[3,5-BIS(METHOXYCARBONYL)PHENOXY]-3-AMINOBENZOATE-->5-hydroxyisophthaldiamide-->1,3diMethyl 5hydroxycyclohexane1,3dicarboxylate
Dacthal METHYL 4-[3,5-BIS(METHOXYCARBONYL)PHENOXY]-3-AMINOBENZOATE 2'-Hydroxy-3-phenylpropiophenone N,N-Dimethylformamide Mono-methyl isophthalate 4-Hydroxyisophthalic acid METHYL-3-NITRO-4-(3,5-DICARBOXYMETHYL-PHENOXY)-BENZOATE 5-Hydroxyisophthalic acid Biphenyl dimethyl dicarboxylate 3-Hydroxybenzoic acid DIMETHYL 5-METHOXYISOPHTHALATE DIMETHYL 5-BENTYLOXY-ISOPHTHALATE Dimethyl 5-hydroxyisophthalate 2,3,4-Trihydroxybenzoic acid Dimethyl isophthalate DIMETHYL 4-HYDROXYISOPHTHALATE 5-HYDROXY-ISOPHTHALIC ACID DIETHYL ESTER Dimethyl terephthalate
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